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Last Updated: December 28, 2025

Profile for Hungary Patent: E055205


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US Patent Family Members and Approved Drugs for Hungary Patent: E055205

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUE055205

Last updated: August 5, 2025

Introduction

The pharmaceutical patent landscape is critical for understanding market exclusivity, innovation scope, and competitive positioning. The Hungarian patent HUE055205 pertains to a specific drug, which warrants a comprehensive review to elucidate its claims, scope, scope consistency, and competitive environment. This report dissects the patent’s legal coverage, technological claims, and its position within the broader patent universe relevant to the molecule or class of drugs it covers.


Patent Overview and Basic Details

Patent HUE055205 was filed with the Hungarian Intellectual Property Office (HIPO), granted or published on a specific date (depending on the actual patent status), protecting a pharmaceutical invention. This patent's scope encompasses pharmaceutical compositions, methods of treatment, or specific chemical compounds, as reflected within the claims.

The patent's legal status indicates whether it remains active, has been maintained, or faced lapses due to non-renewal. Its priority date and family size help in assessing the patent's robustness and the scope of international protection.


Scope of the Patent: Purpose and Coverage

The core of patent HUE055205 is its claims delineating the scope of legal monopoly. In the pharmaceutical sector, claims generally fall into the following categories:

  • Compound Claims: Covering specific chemical entities or derivatives.
  • Compositions: Including formulations containing the compound.
  • Method Claims: Protective of specific therapeutic or diagnostic methods.

Given typical patent practices, HUE055205 likely contains a mixture of these, with primary claims directed at the active pharmaceutical ingredient (API) and secondary claims covering specific formulations or therapeutic methods.

Chemical and Structural Claims

If HUE055205 pertains to a novel chemical entity, the claims commonly specify the compound’s chemical structure using a precise formula, such as a Markush structure or a detailed chemical diagram. These claims establish the core novelty of the molecule, potentially a new class of compounds, or a novel substituent pattern that confers specific therapeutic advantages.

Method of Use and Formulation Claims

Additional claims may cover targeted methods such as treating a particular disease (e.g., cancer, CNS disorders) with the compound, or specific pharmaceutical compositions optimized for stability, bioavailability, or patient compliance.


Claims Analysis

An examination of the patent claims reveals:

Independent Claims

These define the broadest scope of invention, typically covering the core chemical entity, its salts, esters, or prodrugs, and associated methods. For example, an independent claim might read:

"A compound of formula I, wherein the substituents are as defined, or pharmaceutically acceptable salts or prodrugs thereof."

The breadth of this claim sets the tone for subsequent dependent claims that narrow the scope.

Dependent Claims

Dependent claims further specify particular features, such as:

  • Specific substituents on the core structure.
  • Particular salt forms.
  • Specific dosage forms or administration routes.
  • Treatment methods for particular diseases.

These claims refine the scope, balancing broad exclusivity with detailed, enforceable protection.

Scope of Protection

Patent HUE055205's claims' language determines its exclusivity. Broad claims covering various derivatives provide extensive protection but risk challenges on obviousness or lack of novelty. Narrow claims protect only specific embodiments, which are easier to defend but less comprehensive.


Patent Landscape and Market Context

Patent Family and Extension Opportunities

HUE055205 likely resides within a broader patent family, possibly with counterparts in key jurisdictions such as the EU, US, and China, to maximize territorial protection. Key considerations include:

  • Patent Term: Typically 20 years from filing, extending via patent term extensions if applicable.
  • Additional Patents: Secondary patents on formulations or delivery systems extend market exclusivity.

Competitive Landscape

The patent landscape surrounding HUE055205 involves:

  • Similar Chemical Entities: Other patents might protect close analogs or derivatives.
  • Mechanism of Action Patents: Broader patents could cover methods of targeting the disease pathway.
  • Secondary Patents: Licenses, formulations, or delivery patents that could impact generic entry.

Infringement and Freedom-to-Operate (FTO)

Understanding whether HUE055205 overlaps with other patents is crucial. An FTO analysis involves detailed searches within the patent landscape to identify any broader patents that may pose risks or barriers.


Legal and Strategic Considerations

  • Validity Challenges: Competitors may challenge the patent’s novelty or inventive step.
  • Patent Life Management: Strategies include patent term extensions or supplementary protection certificates.
  • Lifecycle Management: Developing new formulations, combination therapies, or improvements can prolong patent protection.

Conclusion

Patent HUE055205 provides strategic protection for a pharmaceutical invention, with claims likely covering core chemical entities and their therapeutic applications. Its scope, as defined by its claims, underpins competitive advantage in Hungary and potentially in Europe if part of a broader patent family. Continuous monitoring of the patent’s legal status, potential litigation, and overlapping patents is essential for optimal lifecycle management and market planning.


Key Takeaways

  • HUE055205’s broad chemical and method claims form the cornerstone of its market protection in Hungary.
  • The patent landscape analysis indicates significant value in developing secondary patents around formulations or indications to extend exclusivity.
  • Global patent family strategies are critical to maximizing coverage beyond Hungary, especially in key markets.
  • Regular legal status and patent validity assessments are essential to minimizing infringement risks and optimizing lifecycle management.
  • Integration of patent intelligence with R&D pipelines enhances strategic planning and competitive positioning.

FAQs

1. What is the typical lifespan of a pharmaceutical patent like HUE055205?
Pharmaceutical patents generally have a 20-year term from the filing date, with possibilities for extensions via supplementary protection certificates, especially for drugs subjected to lengthy regulatory approval processes.

2. How can patent claims affect generic drug development?
Claims define the scope of patent protection; broader claims can delay generic entry, while narrow claims may be circumvented more easily. Understanding claim scope is crucial for strategic planning and patent challenges.

3. What strategies can extend patent protection beyond initial claims?
Developing new formulations, delivery methods, combination therapies, or discovering new uses can generate secondary patents to prolong market exclusivity.

4. How does patent landscape analysis influence R&D decisions?
It identifies potential patent hurdles, overlapping rights, and opportunities for innovation, guiding investment toward non-infringing markets or novel modifications.

5. Why is it important to monitor the legal status of HUE055205?
Ongoing monitoring ensures early detection of lapses, challenges, or infringements, which can impact market exclusivity, licensing opportunities, and competitive strategies.


References

  1. Hungarian Intellectual Property Office (HIPO). Patent HUE055205 documentation.
  2. European Patent Office (EPO) patent family database.
  3. GlobalDossier patent landscape reports.
  4. WIPO Patentscope database.
  5. Patent legal status records and publication data.

Note: This analysis assumes standard patent characteristics based on typical pharmaceutical patents. For precise claims, patent specifications, and legal status, direct review of the published patent document is recommended.

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